Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: PHOX2B-AS1 (Hsa)
(GRCh38)4:41748428C>A
(Homo sapiens)Allele/Variant
Source: rs1733981524
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748428C>A
(GRCh38)4:41748439G>A
(Homo sapiens)Allele/Variant
Source: rs774739194
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748439G>A
(GRCh38)4:41748446G>A
(Homo sapiens)Allele/Variant
Source: rs762144117
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748446G>A
(GRCh38)4:41748449C>A
(Homo sapiens)Allele/Variant
Source: rs1262122327
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748449C>A
(GRCh38)4:41748364C>A
(Homo sapiens)Allele/Variant
Source: rs776614949
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748364C>A
(GRCh38)4:41748393T>C
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748393T>C
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748393T>C
(GRCh38)4:41748387C>T
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748387C>T
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748387C>T
(GRCh38)4:41748536G>T
(Homo sapiens)Allele/Variant
Source: rs1733986571
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748536G>T
(GRCh38)4:41748427G>C
(Homo sapiens)Allele/Variant
Source: rs1458869707
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748427G>C
(GRCh38)4:41748505A>C
(Homo sapiens)Allele/Variant
Source: rs1733985004
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748505A>C
(GRCh38)4:41748458A>C
(Homo sapiens)Allele/Variant
Source: rs1012348354
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748458A>C
(GRCh38)4:41748412G>A
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748412G>A
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748412G>A
(GRCh38)4:41748466T>A
(Homo sapiens)Allele/Variant
Source: rs2153113059
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748466T>A
(GRCh38)4:41748466T>C
(Homo sapiens)Allele/Variant
Source: rs2153113059
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748466T>C
(GRCh38)4:41748569G>T
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748569G>T
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748569G>T
(GRCh38)4:41748416G>T
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748416G>T
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748416G>T
(GRCh38)4:41748404G>A
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748404G>A
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748404G>A
(GRCh38)4:41748454C>A
(Homo sapiens)Allele/Variant
Source: rs1733982922
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748454C>A
(GRCh38)4:41748464G>T
(Homo sapiens)Allele/Variant
Source: rs2153113058
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748464G>T
(GRCh38)4:41748355G>A
(Homo sapiens)Allele/Variant
Source: rs201073251
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748355G>A
(GRCh38)4:41748490C>T
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748490C>T
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748490C>T
(GRCh38)4:41748608C>T
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748608C>T
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, start_lost, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748608C>T
(GRCh38)4:41748417C>A
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748417C>A
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748417C>A
(GRCh38)4:41748375G>A
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748375G>A
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748375G>A
(GRCh38)4:41748511T>A
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748511T>A
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748511T>A
(GRCh38)4:41748453G>T
(Homo sapiens)Allele/Variant
Source: rs1488529123
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748453G>T
(GRCh38)4:41748559T>C
(Homo sapiens)Allele/Variant
Source: rs968453180
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748559T>C
(GRCh38)4:41748537C>G
(Homo sapiens)Allele/Variant
Source: rs2153113067
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748537C>G
(GRCh38)4:41748537C>T
(Homo sapiens)Allele/Variant
Source: rs2153113067
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748537C>T
(GRCh38)4:41748550T>G
(Homo sapiens)Allele/Variant
Source: rs780786684
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748550T>G
(GRCh38)4:41748541A>G
(Homo sapiens)Allele/Variant
Source: rs200971068
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748541A>G
(GRCh38)4:41748455C>A
(Homo sapiens)Allele/Variant
Source: rs1577561242
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748455C>A
(GRCh38)4:41748715C>T
(Homo sapiens)Allele/Variant
Source: rs538445545
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748715C>T
(GRCh38)4:41748477T>C
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748477T>C
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748477T>C
(GRCh38)4:41748376C>A
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748376C>A
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748376C>A
(GRCh38)4:41748561C>T
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748561C>T
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748561C>T
(GRCh38)4:41748562A>G
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748562A>G
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748562A>G
(GRCh38)4:41748582T>C
(Homo sapiens)Allele/Variant
Source: rs1255325771
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748582T>C
(GRCh38)4:41748588T>C
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748588T>C
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, splice_donor_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748588T>C
(GRCh38)4:41748418A>T
(Homo sapiens)Allele/Variant
Source: rs1733981070
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748418A>T
(GRCh38)4:41748519G>C
(Homo sapiens)Allele/Variant
Source: rs1733985532
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748519G>C
(GRCh38)4:41748535G>C
(Homo sapiens)Allele/Variant
Source: rs1358966233
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748535G>C
(GRCh38)4:41748555G>C
(Homo sapiens)Allele/Variant
Source: rs1353983410
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748555G>C
(GRCh38)4:41748475G>A
(Homo sapiens)Allele/Variant
Source: rs1553898221
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748475G>A
(GRCh38)4:41748577A>G
(Homo sapiens)Allele/Variant
Source: rs577333579
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748577A>G
(GRCh38)4:41748425C>G
(Homo sapiens)Allele/Variant
Source: rs763699416
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748425C>G
(GRCh38)4:41748407G>T
(Homo sapiens)Allele/Variant
Source: rs1235634555
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748407G>T
(GRCh38)4:41748425C>A
(Homo sapiens)Allele/Variant
Source: rs763699416
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748425C>A
(GRCh38)4:41748410C>G
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748410C>G
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748410C>G
(GRCh38)4:41748535G>A
(Homo sapiens)Allele/Variant
Source: rs1358966233
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748535G>A